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Traditional genomic analysis relies on linear references, which do not accurately represent the diversity of human genomes, particularly for individuals of non-European ancestry. Reference Bias means important genomic variation in clinical research cohorts remains hidden in traditional NGS data analysis. With the right tools, we can overcome these limitations and unlock the full pre-clinical and clinical potential of genomic data. Join us for our upcoming webinar, “Accelerating Drug Discovery: How GRAF Pangenomes Enable Enhanced Insights from Sequencing Data,” and discover the future of NGS analysis efficiency. Together, let's propel genomic research forward towards a more inclusive and impactful future. 🔸 Save the Date: April 3 🔸 Join us at 11:00 AM EDT Secure your spot today! https://lnkd.in/gv9pVTDa #EraofVelsera #NGS #GRAF #DrugDiscovery

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